• 沒有找到結果。

第五章 研究討論

5.3 幾丁聚醣之角色

幾丁質及其衍生物(如幾丁聚醣)在醫學上的研究顯示有許多的功能,例 如,增強免疫能力、抑制腫瘤、降低膽固醇等;而其在醫材上的應用主要有

46

以下的作用【68】:

一、穩定藥物中的成份

幾丁聚醣具有正電荷可以與藥物中帶負電荷游離脂肪交互作用成乳 劑狀,在這種狀態下的幾丁聚醣與脂肪能形成聚合物(co-polymer)有效的 保護脂肪功能性,以避免藥物中脂肪在高溫滅菌過程中遭到破壞。

二、促進藥物的吸收

研究顯示一些不易被吸收的藥物如atenolol 與幾丁聚醣混合後,經實 驗證明幾丁聚醣可以提升 atenolol 被腸道細胞(Caco-2)的吸收率達 10 到 15 倍。

三、延緩或控制藥物的溶解速度

有些藥物是水溶性或是遇到酸隨即溶解,使得這些藥物無法達到小 腸被吸收而喪失其功效,因此延緩或控制藥物的溶解速率是相當的重 要。經過處理過的幾丁聚醣以不同比例與高水溶性的藥物混合做成錠片 後能有效的延長其溶解時間。

四、幫助藥物送達目的器官

幾丁聚醣具有疏水基與親水基兩種官能基,使得幾丁聚醣能與紫杉 醇(taxol)形成小於 100 nm 的小顆粒膠粒(micelle),經實驗發現這種形式的 紫杉醇更能有效地送達腫瘤部位,而且與幾丁聚醣混合紫杉醇對腫瘤細 胞的抑制能力較游離態紫杉醇的功效好。

曾有研究指出幾丁聚醣有抑菌的功能,其抑菌機轉有二:一為幾丁聚醣因 具有帶正電陽離子的特性,可和黴菌細胞表面的陰離子結合,導至黴菌細胞 膜的通透性改變,使黴菌細胞內蛋白質,紫外線吸收物質及電解質滲漏而死 亡。 另一抑菌機轉則是幾丁聚醣可藉由甲殼素酵素(chitinase)水解,使其分

子量變小而穿透細菌的細胞核並且和細菌的 DNA 相互反應,來抑制細菌的

mRNA 合成達到抑菌的效果。本研究中發現不論是否交聯的幾丁聚醣海綿底 體,對本實驗所採用之兩種常見之標準細菌均無抑菌效果,唯其真正原因仍

47

有待進一步研究。

本研究中之幾丁聚醣海綿體是立體的構造,雖因經交聯後產生不規則及 表面皺摺之情況,但仍顯示可攜帶並穩定釋放抗生素,且由SEM 觀察到其所 呈現之立體架構,如以往研究所指出的【4、26、28、33、42、44、53、92、

93】,應有利於細胞接觸及生長。

48

第六章 結論

經三聚磷酸交聯後之含有四環黴素之幾丁聚醣結構架體可穩定持續釋放

四環黴素至11 天。因此,我們認為,以含有四環黴素之幾丁聚醣海綿體經三

聚磷酸交聯後可以作為牙周炎治療之材料,總結其特點如下:

一、具生物相容性,可被人體吸收

二、可有效的攜帶及穩定的釋放藥物,並有較長的釋放時間 三、抑菌效果明顯

四、立體架構有利於組織再生工程 五、預期具有臨床操作簡易性 六、具創新性及廣泛應用之潛力

唯其應用於醫療之實際效果,仍有待更進一步之生物體研究。如前述本 研究之限制所言,後續研究應以不同模式之幾丁聚醣、不同濃度之四環黴素、

不同之抗生素及針對牙周致病菌為研究標的。

49

參考文獻

1. 王三郎(1996),「水產資源利用學」,高立圖書公司,第 87-94 頁。

2. 江晃榮(1996),「新生技產品:幾丁質、幾丁聚醣產業現況與展望」,財團 法人生物技術開發中心,第41 頁。

3. Allen CR and Hadwiger LA (1979), “The Fungicidal Effect of Chitosan on Fungi of Varying Cell Wall Composition,” Experimental Mycology, Vol. 3, No.

10, pp. 285-287.

4. Anitua E. (1999), “Plasma Rich in Growth Factors: Preliminary Results of Use in The Preparation of Future Sites for Implants,” International Journal of Oral Maxillofacial Implants, Vol. 14, No. 4, pp. 529-535.

5. Aydin Z, Akbuga J. (1996), “Chitosan Beads for the Delivery of Salmon Calcitonin: Preparation and Characteristics,” International Journal of Pharmacology, Vol. 131, No. 6, pp. 101-103.

6. Baker PJ, Evans RT, Slots J, Genco RJ (1985), “Susceptibility of Human Oral Anaerobic Bacteria to Antibiotics Suitable for Topical Use,” Journal of Clinic Periodontology, Vol. 12, No. 3, pp. 201-208.

7. Bollen CML, Quirynen M. (1996), “Microbiological Response to Mechanical Treatment in Combination with Adjunctive Therapy: A Review of the Literature,” Journal of Periodontology, Vol. 67, No. 11, pp. 1143-1158.

8. Calvo P, Remunan-Lopez C, Vila-Jato JL, Alonso MJ. (1997), “Chitosan and Chitosan / Ethylene Oxide-propylene Oxide Block Copolymer Nanoparticles as Novel Carriers for Proteins and Vaccines,” Pharmacology Research, Vol. 14, No. 10, pp. 1431-1436.

9. Calvo P, Remunan-Lopez C, Vila-Jato JL, Alonso MJ. (1998), “Novel Hydrophilic Chitosan-Polyethylene Oxide Nanoparticles as Protein Carriers,”

Journal of Applied Polymer Science, Vol. 63, No. 4. pp. 125-132.

10. Cattabriga M, Pedrazzoli V, Cattabriga A, et al (1996), “Tetracycline Fiber Used Alone or with Scaling and Root Planning in Periodontal Maintenance Patients: Clinical Results,” Quintessence International, Vol. 27, No. 6, pp.

395-400.

11. Chung TW, Lu YF, Wang SS, Lin YS, Chu SH (2002), “Growth of Human

50

Endothelial Cells on Photochemically Grafted Gly-Arg-Gly-Asp (GRGD) Chitosans,” Biomaterials, Vol. 23, No. 24, pp. 4803-4809.

12. Ciancio SG, Cobb CM, Leung M (1992), “Tissue Concentration and Localization of Tetracycline Following Site Specific Tetracycline Fiber Therapy,” Journal of Periodontology, Vol. 63, No. 10, pp. 849-852.

13. Correa JU, Elango I, Polacheck E (1982), “Endo-chitinase, a Mannan-associate Enzyme from Saccharoment Cerevisiae,” Journal of Biological Chemistry, Vol. 257, No. 3, pp. 1392-1397.

14. Cosio IG, Fisher RA, Carroad DA (1982), “Bioconversion of Shellfish Chitin Waste: Waste Pretreatment, Enzyme Protection, Process Design, and Economic Analysis,” Journal of Food Science, Vol. 47, No. 6, pp. 901-905.

15. Cutright DE, Colonel, Bhaskar SN, General B, Beady JM, Colonel L, Getter L, Posey WR (1972), “Reaction of Bone to Tricalcium Phosphate Ceramic Pellets,” Oral Surgery, Vol. 33, No. 5, pp. 851-856.

16. Deshpande MV (1986), “Enzyme Degradation of Chitin and Its Biological Application,” Journal of Science and Industry Research, Vol. 45, No. 3, pp.

273-277.

17. Drisko CL, Cobb CM, Killoy WJ, et al (1995), “Evaluation of Periodontal Treatments Using Controlled-release Tetracycline Fibers: Clinical Response,”

Journal of Periodontology, Vol. 66, No. 8, pp. 672-691.

18. Flemmig TF, Weinacht S, Rudiger S, Rumetsch M, Jung A, Klaiber B (1996),

“Adjunctive Controlled Topical Application of Tetracycline HCl in the Treatment of Localized Persistent or Recurrent Periodontitis: Effects on Clinical Parameters and Elastase-alphal-proteinase Inhibitor in Gingival Crevicular Fluid,” Journal of Clinical Periodontology, Vol. 23, No. 3 pt 1, pp.

914-921.

19. Goodson JM, Cugini MA, Kent RL, et al (1991), “Multicenter Evaluation of Tetracycline Fiber, II. Clinical Response,” Journal of Periodontal Research, Vol. 26, No. 4, pp. 371-379.

20. Goodson JM, Hogan P, Dunham S (1985), “Clinical Responses Following Periodontal Treatment by Local Drug Delivery,” Journal of Periodontology, Vol. 56, No. 11 suppl, pp. 81-87.

21. Goodson HM, Holborow D, Dunn RL, Hogan P, Dunham S (1983),

51

“Monolithic Tetracycline-containing Fibers for Controlled Delivery to Periodontal Pockets,” Journal of Periodontology, Vol. 54, No. 7, pp. 575-579 22. Goodson JM, Tanner A (1992), “Antibiotic Resistance of the Subgingival

Microbiota Following Local Tetracycline Therapy,” Oral Microbiological Immunology, Vol. 7, No. 2, pp. 113-117.

23. Goodson JM, Tanner A, McArdle S, Dix K, Watanabe SM (1991),

“Multicenter Evaluation of Tetracycline Fiber Therapy. III. Microbiology Response,” Journal of Periodontal Research, Vol. 26, No. 5, pp. 440-451.

24. Gordon J, Walker C, Hovliaras C, Socransky S (1990), “Efficacy of Clindamycin Hydrochloride in Refractory Periodontitis: 24-month Results,”

Journal of Periodontology, Vol. 61, No. 11, pp. 686-691.

25. Greenstein G, Poison A (1998), “The Role of Local Drug Delivery in the Management of Periodontal Disease: A Comprehensive Review,” Journal of Periodontology, Vol. 69, No. 5, pp. 507-520.

26. Guo JF, Jourdian GW, McCallum DK (1989), “Culture and Growth Characteristics of Chondrocytes Encapsulated in Alginate Beads,” Connect Tissue Research, Vol. 19, No. 2-4, pp. 277-297.

27. Heiji L, Dahlen G, Sundin Y, Wenander A, Goodson JM (1991), “A 4-quadrant Comparative Study of Periodontal Treatment Using Tetracycline-containing Drug Delivery Fibers and Scaling,” Journal of Clinical Periodontology, Vol.

18, No. 2, pp. 111-116.

28. Ishihara M, Ono K, Sato M, et al (2001), “Acceleration of Wound Contraction and Healing with a Photocrosslinkable Chitosan Hydrogel,” Wound Repair Regeneration, Vol. 9, No. 6, pp. 513-521.

29. Ito M (1991), “In Vitro Properties of a Chitosan – Bonded Hydroxyapatite Bone – Filling Paste,” Biomaterials, Vol. 14, No. 1, pp. 41-45.

30. Jameela SR, Jayadrishnan (1995),”A. Glutaraldehyde Cross-linked Chitosan Microspheres as a Long Acting Biodegradable Drug Delivery Vehicle: Studies on the In Vitro Release of Mitoxantrone and In Vivo Degradation of Microspheres in Rat Muscle,” Biomaterials, Vol. 16, No. 10, pp. 769-775.

31. Jameela SR, Kumary TV, Lal AV, Jayakrishnan A (1998),

“Progesterone-loaded Chitosan Microspheres: A long Acting Biodegradable Controlled Delivery System,” Journal of Control Release, Vol. 52, No. 1-2, pp.

52

17-24.

32. Jameela SR, Misra A, Jayakrishnan A (1994), “Cross-linked Chitosan Microspheres as Carriers for Prolonged Delivery of Macromolecular Drugs,”

Journal of Biomaterial Science Polymer Edition, Vol. 6, No. 7, pp: 621-632.

33. Kawase M, Michibayashi N, Nakashima Y, Kurikawa N, Yagi K, Mizoguchi T (1997), “Application of Glutaraldehyde-crosslinked Chitosan as a Scaffold for Hepatocyte Attachment,” Biology Pharmacology Bulletin, Vol. 20, No. 6, pp.

708-710.

34. Kawashima Y, Handa T, Kasai A, Takenaka H, Lin SY, Ando Y (1985), “Novel Method for the Preparation of Controlled-release theophylline Granules Coated with a Polyelectrolyte Complex of Sodium Polyphosphate-chitosan,”

Journal of Pharmacology Science, Vol. 74, No. 3, pp. 264-268.

35. Kawashima Y, Handa T, Kasai A, Takenaka H, Lin SY (1985), “The Effects of Thickness and Hardness of the Coating Film on the Drug Release Rate of theophylline Granules Coated with Chitosan-sodium Tripolyphosphate Complex,” Chemistry Pharmacology Bulletin (Tokyo), Vol. 33, No. 6, pp.

2469-2474.

36. Kerry G. (1994), “Tetracyclne-loaded Fibers as Adjunctive Treatment in Periodontal Disease,” Journal of Academy of Dental Association, Vol. 125, No.9, pp. 199-203

37. Killoy WJ (1998), “The Use of Locally Delivered Chlorhexidine in the Treatment of Periodontitis: Clinical Results,” Journal of Clinical Periodontology, Vol. 25, No. 11 pt 2, pp. 953-958.

38. Klokkevold PR, Lew DS, Ellis DG, Bertolami NC (1991), “Effect of Chitosan on Lingual Hemostasis in Rabbit,” Journal of Oral Maxillofacial Surgery, Vol.

49, No. 8, pp. 858-863.

39. Klokkevold Pr. Subar P, Fukayama H, Bertolami NC (1992), “Effect of Chitosan on Lingual Hemostasis in Rabbit with Platelet Dysfunction induce by Epoprostenol,” Journal of Oral Maxillofacial Surgery, Vol. 50, No. 1, pp.

41-45.

40. Klokkevold PR, Vandemark L, Kenney EB, Bernard GW (1996),

“Osteogenesis Enhanced by Chitosan (Poly-N-Acetyl Glucosaminoglycan) in Vitro,” Journal of Periodontology, Vol.67, No. 11, pp. 1170-1175.

53

41. Knorr D (1984), “Use of Chitinous Polymer in Food,” Food Technology, Vol.

1, No. 1, pp. 87-94.

42. Koyano T, Minoura N, Nagura M, Kobayashi K (1998), “Attachment and Growth of Cultured Fibroblast Cells on PVA/Chitosan-blended Hydrogels,”

Journal of Biomedical Material Research, Vol. 39, No. 3, pp. 486-490.

43. Kratz G, Arnander C, Swedenborg J, Back M, Falk C, Gouda I, Larm O (1997),

“Heparin – Chitosan Complexes stimulate Wound Healing in Human Skin,”

Scadinnavian Journal of Plastic Reconstructive Surgery and Hand Surgery, Vol.

31, No. 2, pp. 119-123.

44. Lee YM, Park YJ, Lee SJ, Ku Y, Han SB, Choi SM, Klokkevold PR, Chung CP (2000), “Tissue Engineered Bone Formation Using Chitosan / Tricalcium Phosphate Sponges,” Journal of Periodontology, Vol. 71, No. 3, pp. 410-417.

45. Lee YM, Park YJ, Lee SJ, Ku Y, Han SB, M, Klokkevold PR, Chung CP (2000), “The Bone Regenerative of Platelet-derived Growth Factor – BB Delivered with a Chitosan / Tricalcium Phosphate Sponge Carrier,” Journal of Periodontology, Vol. 71, No. 3, pp. 418-424.

46. Liu LS, Liu SQ, Ng SY, Froix M, Ohno T, Heller J (1997), “Controlled Release of Interleukin-2 for Tumor Immunotherapy Using Alginate / Chitosan Porous Microspheres,” Journal of Controlled Release,Vol. 43, No. 1, pp.

65-74.

47. Lowenguth RA, Chin I, Caton JG, et al (1995), “Evaluation of Periodontal Treatments Using Controlled-release Tetracycline Fibers: Microbiological Responses,” Journal of Periodontology, Vol. 66, No. 8, pp. 700-707.

48. Lu HK, Lee SY, Lin FP (1998), “Elastic Modulus, Permeation Time and Swelling Ratio of a New Porcine Dermal Collagen Membrane,” Journal of Periodontal Research, Vol. 33, No.5, pp. 243-248.

49. Malette WG, Quigley HJ, Gaines RD, Hohnson ND, Rainer WG (1983),

“Chitosan: A New Hemostatic,” The Annuals of Thoracic Surgery, Vol. 36, No.

1, pp. 55-58.

50. Mandell RL, Tripodi L, Savitt E, Goodson J, Socransky S (1986), “The Effect of Treatment on Actinobacillus Actinomyceterncomitans in Localized Juvenile Periodontitis,” Journal of Periodontology, Vol. 57, No. 2, pp. 94-97.

51. Michalowicz BS, Pihistrom BL, Drisko CL, et al (1995), “Evaluation of

54

Periodontal Treatments Using Controlled-release Tetracycline Fibers : maintenance Response,” Journal of Periodontology, Vol. 66, No. 8, pp.

708-715.

52. Miyake Y, Tsuruda K, Okuda K, Widowati, Iwamoto Y, Suginaka H (1995),

“In Vitro Activity of Tetracyclines Macrolides, Quinolones, Clindamycin and Metronidazole Against Periodontopathic Bacteria,” Journal of Periodontal Research, Vol. 30, No. 4, pp. 290-293.

53. Mizuno K, Yamamura K, Yano K, et al (2003), “Effect of Chitosan Film Containing Basic Fibroblast Growth Factor on Wound Healing in Genetically Diabetic Mice,” Journal of Biomedical Material Research Part A, Vol. 64, No.

1, pp. 177-181.

54. Mombelli A, Lehmann B, Tonetti M, et al (1997), “Clinical Response to Local Delivery of Tetracycline in Relation to Overall and Local Conditions,” Journal of Clinical Periodontology, Vol. 24, No. 7, pp. 470-477.

55. Mombelli A, Tonetti M, Lehmann B, Lang NR (1996), “Topographic Distribution of Black-pigmenting Anaerobes Before and After Periodontal Treatment by Local Delivery of Tetracycline,” Journal of Clinical Periodontology, Vol. 23, No. 10, pp. 906-913.

56. Moses O, Nemcovsky CE, Tal H, Zohar R (2001), “Tetracycline Modulates Collagen Membrane Degradation in Vitro,” Journal of Periodontology, Vol. 72, No. 11, pp. 1588-1593.

57. Muller HP, Eickholz P, Heinecke A, Polil S, Juller RF, Lange DE (1995),

“Simultaneous Isolation of Actinobacillus Actinomyceterncomitans from Subgingival and Extracrevicular Locations of The Mouth,” Journal of Clinical Periodontology, Vol. 22, No. 5, pp. 413-419.

58. Muzzarelli R, Tarsi R, Filippini O, Giovanetti E, Biagini G, Varaldo PE (1990),

“Antimicrobial Properties of N-Carboxybutyl Chitosan,” Antimicrobial Agent and Chemotherapy, Vol. 34, No. 10, pp. 2019-2023.

59. Muzzarelli RAA, Belmonte MM, Tietz C, Biagini R, Ferioli G, Brunelli MA, Fini M, Giardino R, Ilari P, Biagini G (1994), “Stimulatory effect on Bone Formation Exerted by a Modified Chitosan,” Biomaterials, Vol. 15, No. 13, pp.

1075-1081.

60. Muzzarelli RAA, Biagini G, Bellardini M, Simonelli L, Castaldini C, Fratto G

55

(1993), “Osteoconduction Exerted by Methylpyrrolidinone Chitosan Used in Dental Surgery,” Biomaterials, Vol. 14, No. 1, pp. 39-43.

61. Muzzarelli RAA, O’brine M, Clowell RR (1987), “A Rapid Test for Chitinase Activity That Uses 4-Methylumbellifery-N-Acetyl-β-D-Glucosamine,”

Applied and Environment Microbiology, Vol. 53, No. 8, pp. 1718-1724.

62. Myken PS (2005), “Seventeen-year Experience with The St. Jude Medical Biocor Procine Bioprosthesis,” Journal of Heart Valve Disease, Vol. 14, No. 4, pp. 486-492.

63. Newman MG, Kornman KS, Doherty FM (1994), “A 6-month Multi-center Evaluation of Adjunctive Tetracycline Fiber Therapy Used in Conjunction with Scaling and Root Planning in Maintenance Patients : Clinical Results.

Journal of Periodontology, Vol. 65, No. 5 suppl, pp. 685-691.

64. Nishi C, Nakajima N, Ikada Y (1995), “In Vitro Evaluation of Cytotoxicity of Diepoxy Compounds Used for Biomaterial Modification,” Journal of Biomedical Material Research, Vol. 29, No. 7, pp. 829-834.

65. Norling T, lading P, Engstrom S, Larsson K, Krog N, Nissen SS (1992),

“Formulation of A Drug Delivery System Based on a Mixture of Monoglycerides and Triglycerides for Use in The Treatment of Periodontal Disease,” Journal of Clinical Periodontology, Vol. 19, No. 9 pt 2, pp.687-692.

66. Odim J, Laks H, Allada V, Child J, Wilson S, Gjertson D (2005), “Results of Aortic Valve-sparing and Restoration with Autologous Pericardial Leaflet Extensions in Congenital Heart Disease,” Annual Thoracic Surgery, Vol. 80, No. 2, pp.647-653.

67. Ozmeric N, et al (2000), “Chitosan Film Enriched with an Antioxidant Agent Taurine in Fenestration Defect,” Journal of Biomedical Material Research, Vol.

51, No. 3, pp. 500-503.

68. Park YJ, Lee JY, Yeom HR, et al (2005), “Injectable polysaccharide Microcapsules for Prolonged Release of Minocycline for The Treatment of Periodontitis,” Biotechnology Letter, Vol. 27, No. 22, pp. 1761-1766.

69. Peluso G, Petillo O, Ranieri M, Santin M, Ambrosio L, Calabro D, Avallone B, Balsamo G (1994), “Chitosan – Mediated Stimulation of Macrophage Function,” Biomaterials, Vol. 15, No. 15, pp. 1215-1220.

70. Peterson LJ, Hupp JR, Tucker MR, Edward E (1993), “Contemproary Oral

56

and Maxillofacial Surgery”, 2nd Edition, pp. 60-64.

71. Polk A, Amsden B, De Yao K, Peng T, Goodson MF (1994), “Controlled Release of Albumin from Chitosan-Alginate Microcapsules,” Journal of Pharmacology Science, Vol. 83, No. 2, pp. 178-185.

72. Rao SB, Sharma CP (1997), “use of Chitosan as a Biomaterial: Studies on Its Safety and Hemostatic Potential,” Journal of Biomedical Materials Research, Vol. 34, No. 1, pp. 21-28.

73. Rapley JW, Cobb CM, Killoy WJ, Williams DR (1992), “Serum Levels of Tetracycline During Treatment with Tetracycline-containing Fibers,” Journal of Periodontology, Vol. 63, No. 10, pp. 817-820.

74. Rifkin BR, Vernillo AT, Golub LM (1993), “Blocking Periodontal Disease progression By Inhibiting Tissue Destructive Enzymes: A Potential Tehrapeutic Role for Tetracyclines and Their Chemically-modified Analogs,”

Journal of Periodontology, Vol. 64, No. 8 suppl, pp. 819-827.

75. Seymur RA, Heasman PA (1995), “Tetracyclines in The Management of Periodontal Disease : A Review,” Journal of Clinical Periodontology, Vol. 22, No. 11, pp. 22-35.

76. Sezer AD, Akbuga J (1995), “Controlled Release of Piroxicam form Chitosan Beads,” International Journal of Pharmacology, Vol. 121, No. 4, pp. 113-116.

77. Shu XZ, Zhu KJ (2000), “A Novel Approach to Prepare Tripolyphosphate / Chitosan Complex Beads for Controlled Release Drug Delivery,” International Journal of Pharmacology, Vol. 201, No. 1, pp. 51-58.

78. Speer DP, Chvapil M, Eskelson CD, Ulrich J (1980), “Biological Effects of Residual Glutaraldehyde in Glutaraldehyde-tanned Collagen Biomaterials,”

Journal of Biomedical Materials Research, Vol. 14, No. 6, pp. 753-764.

79. Stanley WL Watter GG, Chan BG, Kelly SH (1976), “Immobilization of Glucose Isomerase on Chitin with Glutaraldehyde and By Simple Adsorption,” Biotechnology and Bioengineering, Vol. 18, No. 10, pp.

439-442.

80. Stone CA, Wright H, Clarke T, Powell R, Dvaraj VS (2000), “Healing at Skin Graft Donor Sites Dresses with Chitosan,” British Journal of Plastic Surgery, Vol. 53, No. 4, pp. 601-606.

81. Tonetti M, Cugini MA, Goodson JM (1990), “Zero Order Delivery with

57

Periodontal Placement of Tetracycline-loaded Ethylene Vinyl Acetate Fibers,”

Journal of Periodontology, Vol. 25, No. 4, pp. 243-249.

82. Tonetti MS, Pini-Prato G, Cortellini P (1994), “Principles and Clinical Applications of Periodontal Controlled Drug Delivery with Tetracycline Fibers,” International Journal of Periodontics Restorative Dentistry, Vol. 14, No. 5, pp. 421-435.

83. Tsai GJ, Su WH (1999), “Antibacterial Activitiy of Shrimp Chitosan Against Escherichia Coli,” Journal of Food Protection, Vol. 62, No. 3, pp. 239-243.

84. Usami Y, Okamoto Y, Takaama T, Shigemasa Y, Minami S (1998), “Chitin and Chitosan Stimulate Canine Polymorphonuclear Cells to Release Leukotriene B4 and Prostaglandin E2,” Journal of Biomedical Materials Research, Vol. 42, No. 4, pp. 517-522.

85. Van Dyke Te, Lester MA Shapira L (1993), “The Role of The Host Response in Periodontal Disease Progression: Implications for Future Treatment Strategies,” Journal of Periodontology, Vol. 64, No. 8 suppl, pp. 792-806.

86. Van Winkelhoff AJ, Herrera Gonzales D, Winkel EG, Dellemijn-Kippuw N, Vandenbroucke-Grauls CM, Sanz M (2000), “Antimicrobial Resistance in The Subgingibval Micorflora in Patients with Adult Periodontitis: A Comparison Between The Netherlands and Spain,” Journal of Clinical Periodontology, Vol.

27, No. 2, pp. 79-86.

87. Van Winkelhoff AJ, Rams TE, Slots J (1996), “Systemic Antibiotic Therapy in Periodontics,” Periodontology 2000, Vol. 10, Feb, pp. 45-78.

88. Vandekerckhove BN, Quirynen M, Van Steenberghe D (1997), “The Use of Tetracycline-containing Controlled-release Fibers in The Treatment of Refractory Periodontitis,” Journal of Periodontology, Vol. 68, No. 4, pp.

353-361.

89. Von Troil-Ljnden B, Saarela M, Matt QJ, Aialuusua S, Jousimies-Somer H, Asikainen S (1996), “Source of Suspected Periodontal Pathogens Re-emerging After Periodontal Treatment,” Journal of Clinical Periodontology, Vol. 23, No.

6, pp. 601-607.

90. Wong MY, Lu CL, Liu CM, Hou LT (1996), “ II. Microbiological Response of Localized Sites with Recurrent Periodontitis in Maintenance Patients Treated with Tetracycline Fibers,” Journal of Periodontology, Vol. 70, No. 8, pp.

相關文件